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Aminomethyltransferase Antikörper (N-Term)

AMT Reaktivität: Human, Maus, Ratte, Hund, Kaninchen, Rind (Kuh), Meerschweinchen, Pferd, Zebrafisch (Danio rerio) WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2785650
  • Target Alle Aminomethyltransferase (AMT) Antikörper anzeigen
    Aminomethyltransferase (AMT)
    Bindungsspezifität
    • 6
    • 4
    • 4
    • 2
    • 2
    • 1
    N-Term
    Reaktivität
    • 23
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Maus, Ratte, Hund, Kaninchen, Rind (Kuh), Meerschweinchen, Pferd, Zebrafisch (Danio rerio)
    Wirt
    • 19
    • 4
    Kaninchen
    Klonalität
    • 21
    • 2
    Polyklonal
    Konjugat
    • 19
    • 2
    • 1
    • 1
    Dieser Aminomethyltransferase Antikörper ist unkonjugiert
    Applikation
    • 18
    • 8
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Sequenz
    QRAVSVVARL GFRLQAFPPA LCRPLSCAQE VLRRTPLYDF HLAHGGKMVA
    Homologie
    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 92%
    Produktmerkmale
    This is a rabbit polyclonal antibody against AMT. It was validated on Western Blot using a cell lysate as a positive control.
    Aufreinigung
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the N terminal region of human AMT
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  • Applikationshinweise
    Optimal working dilutions should be determined experimentally by the investigator.
    Kommentare

    Antigen size: 403 AA

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    Aminomethyltransferase (AMT)
    Andere Bezeichnung
    AMT (AMT Produkte)
    Synonyme
    F16J13.200 antikoerper, F16J13_200 antikoerper, T7P1.13 antikoerper, T7P1_13 antikoerper, wu:fc31f04 antikoerper, wu:fd44b12 antikoerper, wu:fd54h12 antikoerper, zgc:103483 antikoerper, zgc:109741 antikoerper, GCE antikoerper, GCST antikoerper, GCVT antikoerper, NKH antikoerper, EG434437 antikoerper, aminomethyltransferase antikoerper, Glycine cleavage T-protein family antikoerper, Aminomethyltransferase antikoerper, aminomethyltransferase L homeolog antikoerper, AMT antikoerper, AT4G12130 antikoerper, AT1G60990 antikoerper, Tb11.01.1440 antikoerper, Palpr_0614 antikoerper, Ocepr_1643 antikoerper, Celal_2914 antikoerper, Deima_1002 antikoerper, Deipr_1956 antikoerper, Bacsa_3405 antikoerper, Celly_0288 antikoerper, Weevi_0527 antikoerper, Fluta_3952 antikoerper, Marky_0785 antikoerper, Spico_1217 antikoerper, Poras_1228 antikoerper, Halhy_3617 antikoerper, amt antikoerper, amt.L antikoerper, Amt antikoerper
    Hintergrund
    The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). Glycine encephalopathy (GCE) may be due to a defect in any one of these enzymes.The enzyme system for cleavage of glycine (glycine cleavage system, EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase, MIM 238300), H protein (a lipoic acid-containing protein, MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase, MIM 238331). Glycine encephalopathy (GCE, MIM 605899) may be due to a defect in any one of these enzymes.[supplied by OMIM]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-2102 D13811.1 1-2102 2103-2117 BC044792.1 3271-3285
    Alias Symbols: GCE, GCST, NKH, GCVT
    Protein Interaction Partner: HSPA8,
    Protein Size: 403
    Molekulargewicht
    44 kDa
    Gen-ID
    275
    NCBI Accession
    NM_000481, NP_000472
    UniProt
    P48728
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